-We use cookies to offer you a better browsing experience, analyze site traffic, and personalize content. Read about how we use cookies and how you can control them by visiting our Cookie Settings page. If you continue to use this site, you consent to our use of cookies. Cookie Settings AllowSearch for Job TitleEnter LocationSearchCountry Approval SpecialistLocation Madrid, Spain Job Id R-01362267 Job Type Full time Category Clinical Research Remote Fully RemoteAdd To Cart Apply Now Share via email Share via Facebook Share via LinkedIn Share via twitter Our team of colleagues in clinical research services are at the forefront of getting cures to market. We bring a high caliber of scientific and clinical expertise to the development of drugs that address the world’s most challenging health concerns. Our Clinical Research team, who powers our PPD® clinical research portfolio, are part of our leading global contract research organization (CRO).Accessibility/Disability Access We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. Learn more Equal Opportunity Policy Statement Thermo Fisher Scientific is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to any characteristic protected by local, state, or federal laws, rules, or regulations.



Learn more Get notified for similar jobsYou'll receive updates once a weekEnter Email address (Required)Activate Manage alerts Get tailored job recommendations based on your interests.Get StartedSimilar Jobs Manager Clinical Operations FSP - EMEA Available in 3 locations Job Id R-01367100 Become part of our team as Manager Clinical Operations – EMEA, leading a team to drive clinical operations excellence. Oversee staff performance, ensure adherence to SOPs, and support project delivery. Ideal for experienced leaders with strong clinical trials monitoring and mentoring skills. Sr/Regulatory Affairs Specialist - FSP - EMEA Available in 6 locations Job Id R-01368383 We are seeking a Regulatory Affairs Specialist to lead the review and approval of essential documents for site activation across multiple countries. You will ensure regulatory compliance and quality, working closely with clients and internal teams. Ideal candidates have experience in regulatory affairs and strong communication skills. CRA (Level II) to Sr CRA (Level II) Available in 2 locations Job Id R-01358166 We are currently hiring a Clinical Research Associate (Level II) to support clinical trial monitoring and site management. You will ensure protocol and regulatory compliance, manage documentation, and collaborate with investigational sites. Ideal candidates have at least two years’ experience in clinical research and strong communication skills. Site Contract Specialist Location Madrid, Spain Job Id R-01363437 We are recruiting a Site Contract Specialist to support the preparation, negotiation, and finalisation of contracts with investigative sites. You will liaise with internal teams and ensure compliance with contractual processes. Idóneo for candidates with a bachelor's degree and up to two years' relevant experience. CRA I/ II- FSP - Spain Available in 2 locations Job Id R-01338542 Join us as a Clinical Research Associate and play a key role in monitoring clinical trials and ensuring regulatory compliance. You will manage site processes, conduct site visits, and support investigational sites. Ideal for candidates with 1–2 years’ CRA experience and a background in oncology studies. Show more

📌 Associate Specialist, Regulatory Affairs (Madrid)
🏢 Abacus Medicine Group
📍 Madrid